Detection of L-Proline-Catalyzed Michael Addition Reaction in Model Biomembrane

A method to detect the L-proline- (L-Pro-) catalyzed Michael addition reaction in model biomembranes has been established, using N-[p(2-benzimidazolyl)phenyl]maleimide and acetone as reactants. The effect of liposome membranes on this reaction was kinetically analyzed using fluorescence spectroscopy...

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Main Authors: Masanori Hirose, Shigenori Sugisaki, Keishi Suga, Hiroshi Umakoshi
Format: Article
Language:English
Published: Hindawi Limited 2019-01-01
Series:Journal of Chemistry
Online Access:http://dx.doi.org/10.1155/2019/4926435
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spelling doaj-b28ba26aa6b9401496bb9bfffb10e4722020-11-24T21:53:30ZengHindawi LimitedJournal of Chemistry2090-90632090-90712019-01-01201910.1155/2019/49264354926435Detection of L-Proline-Catalyzed Michael Addition Reaction in Model BiomembraneMasanori Hirose0Shigenori Sugisaki1Keishi Suga2Hiroshi Umakoshi3Division of Chemical Engineering, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama-cho, Toyonaka, Osaka 560-8531, JapanDivision of Chemical Engineering, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama-cho, Toyonaka, Osaka 560-8531, JapanDivision of Chemical Engineering, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama-cho, Toyonaka, Osaka 560-8531, JapanDivision of Chemical Engineering, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama-cho, Toyonaka, Osaka 560-8531, JapanA method to detect the L-proline- (L-Pro-) catalyzed Michael addition reaction in model biomembranes has been established, using N-[p(2-benzimidazolyl)phenyl]maleimide and acetone as reactants. The effect of liposome membranes on this reaction was kinetically analyzed using fluorescence spectroscopy. The kinetics of the reaction were different from those of the constituent lipids of the liposomes. Zwitterionic 1,2-dipalmitoyl-sn-glycero-3-phosphocholine liposome, which is in the solid-ordered phase, had a better value of reaction rate, suggesting that the reaction rate constants of this reaction in liposome membrane systems could be regulated by the characteristics of the liposome membrane (i.e., the phase state and surface charge). Based on the results obtained, a plausible model of the L-Pro-catalyzed Michael addition reaction was discussed. The obtained results provide us with an easily detectable method to assess the reactivity of L-Pro in biological systems.http://dx.doi.org/10.1155/2019/4926435
collection DOAJ
language English
format Article
sources DOAJ
author Masanori Hirose
Shigenori Sugisaki
Keishi Suga
Hiroshi Umakoshi
spellingShingle Masanori Hirose
Shigenori Sugisaki
Keishi Suga
Hiroshi Umakoshi
Detection of L-Proline-Catalyzed Michael Addition Reaction in Model Biomembrane
Journal of Chemistry
author_facet Masanori Hirose
Shigenori Sugisaki
Keishi Suga
Hiroshi Umakoshi
author_sort Masanori Hirose
title Detection of L-Proline-Catalyzed Michael Addition Reaction in Model Biomembrane
title_short Detection of L-Proline-Catalyzed Michael Addition Reaction in Model Biomembrane
title_full Detection of L-Proline-Catalyzed Michael Addition Reaction in Model Biomembrane
title_fullStr Detection of L-Proline-Catalyzed Michael Addition Reaction in Model Biomembrane
title_full_unstemmed Detection of L-Proline-Catalyzed Michael Addition Reaction in Model Biomembrane
title_sort detection of l-proline-catalyzed michael addition reaction in model biomembrane
publisher Hindawi Limited
series Journal of Chemistry
issn 2090-9063
2090-9071
publishDate 2019-01-01
description A method to detect the L-proline- (L-Pro-) catalyzed Michael addition reaction in model biomembranes has been established, using N-[p(2-benzimidazolyl)phenyl]maleimide and acetone as reactants. The effect of liposome membranes on this reaction was kinetically analyzed using fluorescence spectroscopy. The kinetics of the reaction were different from those of the constituent lipids of the liposomes. Zwitterionic 1,2-dipalmitoyl-sn-glycero-3-phosphocholine liposome, which is in the solid-ordered phase, had a better value of reaction rate, suggesting that the reaction rate constants of this reaction in liposome membrane systems could be regulated by the characteristics of the liposome membrane (i.e., the phase state and surface charge). Based on the results obtained, a plausible model of the L-Pro-catalyzed Michael addition reaction was discussed. The obtained results provide us with an easily detectable method to assess the reactivity of L-Pro in biological systems.
url http://dx.doi.org/10.1155/2019/4926435
work_keys_str_mv AT masanorihirose detectionoflprolinecatalyzedmichaeladditionreactioninmodelbiomembrane
AT shigenorisugisaki detectionoflprolinecatalyzedmichaeladditionreactioninmodelbiomembrane
AT keishisuga detectionoflprolinecatalyzedmichaeladditionreactioninmodelbiomembrane
AT hiroshiumakoshi detectionoflprolinecatalyzedmichaeladditionreactioninmodelbiomembrane
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